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Schlotter, Beate
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1

Location matters – Genotype-phenotype correlation in LRSAM1..:

Reilich, Peter ; Schlotter, Beate ; Montagnese, Federica...
Neuromuscular Disorders.  31 (2021)  2 - p. 123-133 , 2021
Link: https://doi.org/10.1016/..
 
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2

Congenital myasthenic syndrome with tubular aggregates caus..:

Guergueltcheva, Velina ; Müller, Juliane S. ; Dusl, Marina...
Journal of Neurology.  259 (2011)  5 - p. 838-850 , 2011
Link: https://doi.org/10.1007/..
 
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3

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscul..:

Senderek, Jan ; Müller, Juliane S. ; Dusl, Marina...
The American Journal of Human Genetics.  88 (2011)  2 - p. 162-172 , 2011
Link: https://doi.org/10.1016/..
 
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4

Mutation screening of the N-myc downstream-regulated gene 1..:

Hunter, Michael ; Bernard, Rafaëlle ; Freitas, Elizabeth...
Human Mutation.  22 (2003)  2 - p. 129-135 , 2003
Link: https://doi.org/10.1002/..
 
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5

Creatine monohydrate in myotonic dystrophy:

Walter, Maggie C. ; Reilich, Peter ; Lochm�ller, Hanns...
Journal of Neurology.  249 (2002)  12 - p. 1717-1722 , 2002
Link: https://doi.org/10.1007/..
 
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6

Phenotypic variability in two brothers with sarcotubular my..:

Müller-Felber, W. ; Schlotter, Beate ; Töpfer, Marcell...
Journal of Neurology.  246 (1999)  5 - p. 408-411 , 1999
Link: https://doi.org/10.1007/..
 
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7

Linkage of a commoner form of recessive amyotrophic lateral..:

Hentati, Afif ; Ouahchi, Karim ; Pericak-Vance, Margaret A....
neurogenetics.  2 (1998)  1 - p. 55-60 , 1998
Link: https://doi.org/10.1007/..
 
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8

Calf enlargement in neuromuscular diseases: a quantitative ..:

Reimers, Carl D. ; Schlotter, Beate ; Eicke, B.Martin.
Journal of the Neurological Sciences.  143 (1996)  1-2 - p. 46-56 , 1996
Link: https://doi.org/10.1016/..
 
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9

Deletion of the LMNA initiator codon leading to a neurogeni..:

Walter, Maggie C. ; Witt, Thomas N. ; Weigel, Beate Schlotter...
Neuromuscular Disorders.  15 (2005)  1 - p. 40-44 , 2005
Link: https://doi.org/10.1016/..
 
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10

Hexosamine Biosynthetic Pathway Mutations Cause Neuromuscul..:

Senderek, Jan ; Müller, Juliane S ; Dusl, Marina...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3035713.  , 2011
Link: http://www.ncbi.nlm.nih...
 
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11

Bi-allelic truncating mutations in VWA1 cause neuromyopathy:

Deschauer, Marcus ; Hengel, Holger ; Rupprich, Katrin...
Brain.  144 (2021)  2 - p. 574-583 , 2021
Link: https://doi.org/10.1093/..
 
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12

Intraepidermal nerve fibre density as biomarker in Charcot–..:

Hartmannsberger, Beate ; Doppler, Kathrin ; Stauber, Julia...
Brain Communications.  2 (2020)  1 - p. , 2020
Link: https://doi.org/10.1093/..
 
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13

The clinical, histologic, and genotypic spectrum ofSEPN1-re..:

Villar-Quiles, Rocio N. ; von der Hagen, Maja ; Métay, Corinne...
Neurology.  95 (2020)  11 - p. , 2020
Link: https://doi.org/10.1212/..
 
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14

Loss of Neurological Disease HSAN-I-Associated Gene SPTLC2 ..:

Wu, Jingxia ; Ma, Sicong ; Sandhoff, Roger...
Immunity.  50 (2019)  5 - p. 1218-1231.e5 , 2019
Link: https://doi.org/10.1016/..
 
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15

Immunvermittelte / inflammatorische und hereditäre Neuropat..:

Schlotter-Weigel, Beate ; Senderek, Jan
Fortschritte der Neurologie · Psychiatrie.  86 (2018)  9 - p. 566-574 , 2018
Link: https://doi.org/10.1055/..
 
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